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Anti-Legionella pneumophila ELISA (IgA)

EUROIMMUN Medizinische Labordiagnostika AG · Model EI 2150-9601 A · UDI-DI 04049016027508

MJH
10
510(k) clearances
5
Adverse events (2 deaths)
3
Recalls
17
Facilities

Recalls

DateFirmReason
2025-07-22Trinity Biotech USAPotential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065 and 066 to contain particulate matter.
2021-10-11Clark Laboratories, Inc.Contamination of the conjugate may cause a pipetting issue which then could lead to an invalid assay
2006-09-29Inverness Medical Professional DiagnosticsMislabeled product: Outer kit label reads NOW Legionella Urinary Antigen Test, inside contains S. pneumonia test pouches

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.